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Human Genetics
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October 11, 2008
Gene symbol: COL11A2. Disease: Otospondylomegaepiphyseal dysplasia
Zehra Oya Uyguner, Hulya Kayserili
The Journal of Clinical Pediatric Dentistry
|
May 7, 2002
Seckel syndrome: report of a case
Figen Seymen, Bahar Tuna, Hulya Kayserili
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
April 23, 2005
18q deletion syndrome associated with autoimmune thyroid disease presenting as hyperthyroidism
Filiz Tutunculer, Feyza Darendeliler, Hulya Gunoz, et al.
Annales De Genetique
|
April 2, 2003
Haploinsufficiency of TBX3 causes ulnar-mammary syndrome in a large Turkish family
Bernd Wollnik, Hulya Kayserili, Oya Uyguner, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
|
October 23, 2012
A novel c.1255G>T (p.D419Y) mutation in SH3BP2 gene causes cherubism in a Turkish family
Nuriye Dinckan, Yeliz Guven, Hulya Kayserili, et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS
|
June 5, 2013
Multiple synostoses syndrome in three members of a family displaying a novel mutation in NOGGIN gene
H Utkan Aydin, Umut Altunoglu, Z Oya Uyguner, et al.
Fetal and Pediatric Pathology
|
January 8, 2024
Prenatal Diagnosis of Crossed Pulmonary Arteries with a Postnatal Diagnosis of CHARGE Syndrome
Funda Oztunc, Riza Madazli, Hakan Erenel, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics
|
September 20, 2008
Orodental findings of a family with lacrimo-auriculo-dento digital (LADD) syndrome
Yeliz Guven, R Ozgur Rosti, E Bahar Tuna, et al.
American Journal of Medical Genetics. Part A
|
November 4, 2004
Further delineation of Frank-ter Haar syndrome
Saskia M Maas, Hulya Kayserili, Jan Lam, et al.
Cranio : the Journal of Craniomandibular Practice
|
February 27, 2009
Craniodentofacial manifestations in Hallermann-Streiff syndrome
E Bahar Tuna, Tonguc Sulun, Ozgur Rosti, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 76) with videos related to
Sort By:
Page
of 8
Human Genetics
|
October 11, 2008
Gene symbol: COL11A2. Disease: Otospondylomegaepiphyseal dysplasia
Zehra Oya Uyguner, Hulya Kayserili
The Journal of Clinical Pediatric Dentistry
|
May 7, 2002
Seckel syndrome: report of a case
Figen Seymen, Bahar Tuna, Hulya Kayserili
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
April 23, 2005
18q deletion syndrome associated with autoimmune thyroid disease presenting as hyperthyroidism
Filiz Tutunculer, Feyza Darendeliler, Hulya Gunoz, et al.
Annales De Genetique
|
April 2, 2003
Haploinsufficiency of TBX3 causes ulnar-mammary syndrome in a large Turkish family
Bernd Wollnik, Hulya Kayserili, Oya Uyguner, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
|
October 23, 2012
A novel c.1255G>T (p.D419Y) mutation in SH3BP2 gene causes cherubism in a Turkish family
Nuriye Dinckan, Yeliz Guven, Hulya Kayserili, et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS
|
June 5, 2013
Multiple synostoses syndrome in three members of a family displaying a novel mutation in NOGGIN gene
H Utkan Aydin, Umut Altunoglu, Z Oya Uyguner, et al.
Fetal and Pediatric Pathology
|
January 8, 2024
Prenatal Diagnosis of Crossed Pulmonary Arteries with a Postnatal Diagnosis of CHARGE Syndrome
Funda Oztunc, Riza Madazli, Hakan Erenel, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics
|
September 20, 2008
Orodental findings of a family with lacrimo-auriculo-dento digital (LADD) syndrome
Yeliz Guven, R Ozgur Rosti, E Bahar Tuna, et al.
American Journal of Medical Genetics. Part A
|
November 4, 2004
Further delineation of Frank-ter Haar syndrome
Saskia M Maas, Hulya Kayserili, Jan Lam, et al.
Cranio : the Journal of Craniomandibular Practice
|
February 27, 2009
Craniodentofacial manifestations in Hallermann-Streiff syndrome
E Bahar Tuna, Tonguc Sulun, Ozgur Rosti, et al.
Page
of 8